ClinVar Miner

Submissions for variant NM_000342.4(SLC4A1):c.2116C>A (p.Leu706Met)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Jiangsu Institute of Hematology, the First Affiliated Hospital of Soochow University RCV002291018 SCV002500008 likely pathogenic Hereditary spherocytosis type 4 2022-03-01 criteria provided, single submitter research
Revvity Omics, Revvity RCV003138099 SCV003821392 uncertain significance not provided 2022-08-29 criteria provided, single submitter clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.